您好，欢迎来到易推广！ 请登录 免费注册

上海陶术生物科技有限公司 主营产品：生物试剂,实验服务等

当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示

企业档案

会员类型：会员

已获得易推广信誉   等级评定
139成长值

(0 -40)基础信誉积累，可浏览访问

(41-90)良好信誉积累，可接洽商谈

(91+  )优质信誉积累，可持续信赖

易推广会员：5年

工商认证 【已认证】

最后认证时间：

注册号： 【已认证】

法人代表： 【已认证】

企业类型：生产商 【已认证】

注册资金：人民币万 【已认证】

产品数：86101

参观次数：3691640

手机网站：http://m.yituig.com/c135739/

旗舰版地址：http://tsbiochem.app17.com

自主品牌

自主品牌

已选条件

  • T75259Baquiloprim；化合物 BaquiloprimBaquiloprim

    Baquiloprim, an antibiotic, functions as a selective inhibitor of bacterial dihydrofolate reductases, exhibiting in vitro bacteriostatic activity against both Gram-negative and Gram-positive bacteria [1] [2].

    价 格：￥电议型 号：T75259产 地：中国大陆

  • T743666BrCaQ-C10-TPP；化合物 6BrCaQ-C10-TPP6BrCaQ-C10-TPP

    6BrCaQ-C10-TPP, a potent inhibitor of the mitochondrial heat shock protein TRAP1, exhibits antiproliferative activity against various human cancer cells, with an IC50 range of 0.008-0.30 μM. Additionally, it induces disturbances in mitochondrial membranes [1].

    价 格：￥电议型 号：T74366产 地：中国大陆

  • T74322DOBAQ；化合物 DOBAQDOBAQ

    DOBAQ, a pH-sensitive cationic lipid, is utilized in the formulation of liposomes for drug delivery applications [1].

    价 格：￥电议型 号：T74322产 地：中国大陆

  • T73845Piperaquine tetraphosphate；化合物 Piperaquine tetraphosphatePiperaquine tetraphosphate

    Piperaquine tetraphosphate, a potent antimalarial agent, demonstrates inhibitory effects against both chloroquine-sensitive and chloroquine-resistant malaria isolates. When combined with dihydroartemisinin, it holds potential for researching chloroquine-resistant malaria [1] [2].

    价 格：￥电议型 号：T73845产 地：中国大陆

  • T73495q-FTAA；化合物 q-FTAAq-FTAA

    q-FTAA, a potential research compound for Alzheimer´s disease (AD), demonstrates binding affinity to Aβ1-42 fibrils and the Alzheimer´s disease PIB binding complex (ADPBC), with EC50 values ranging from 330-630 nM and 300-500 nM, respectively.

    价 格：￥电议型 号：T73495产 地：中国大陆

  • T7310Paquinimod；帕奎莫德ABR 25757；帕奎莫德|||ABR 25757

    Paquinimod (ABR 25757) is a specific S100A8/S100A9 inhibitor with oral activity. Paquinimod has immunomodulatory activity and can be used for the treatment of systemic lupus erythematosus.

    价 格：￥电议型 号：T7310产 地：中国大陆

  • T73055(S)-VQW-765；化合物 (S)-VQW-765(S)-AQW-051；(S)-AQW-051

    (S)-VQW-765 ((S)-AQW-051) is an orally active, selective, and effective partial agonist of the α7 nicotinic acetylcholine receptor (nAChR), with potential applications in treating cognitive disorders associated with neurological diseases, including Alzheimer´s disease and schizophrenia.

    价 格：￥电议型 号：T73055产 地：中国大陆

  • T71635Murayaquinone；化合物 MurayaquinoneMurayaquinone

    Murayaquinone is a hepatitis C virus proteinase inhibitor and small molecule antagonist of the oncogenic Tcf/β-catenin protein complex.

    价 格：￥电议型 号：T71635产 地：中国大陆

  • T71599AqB007；化合物 AqB007AqB007

    AqB007 is a selective blocker of the Aquaporin-1 ion channel conductance, thereby slowing cancer cell migration.

    价 格：￥电议型 号：T71599产 地：中国大陆

  • T71598AqB011；化合物 AqB011AqB011

    AqB011 is a selective blocker of the Aquaporin-1 ion channel conductance, slowing cancer cell migration.

    价 格：￥电议型 号：T71598产 地：中国大陆

  • T712964-Aaqb；化合物 4-Aaqb4-Aaqb

    4-Aaqb, also known as OB-318, is a natural inhibitor of the autophagy pathway, enhancing immune function, suppressing MAPK and NFκB, showing anti-inflammatory, hypoglycemic, vasorelaxative, and antiproliferative activities.

    价 格：￥电议型 号：T71296产 地：中国大陆

  • T7106Menaquinone-4；四烯甲萘醌Vitamin K2|||Menaquinone K4；四烯甲萘醌|||Vitamin K2|||Menaquinone K4

    Menaquinone-4 (Vitamin K2) is a vitamin K compound used as a hemostatic agent, and also as adjunctive therapy for the pain of osteoporosis.

    价 格：￥电议型 号：T7106产 地：中国大陆

  • T70902AQ-101；化合物 AQ-101AQ-101

    AQ-101 is a inhibitor of MDM2, which induces MDM2 protein degradation through a self-ubiquitination and proteasome-mediated mechanism.

    价 格：￥电议型 号：T70902产 地：中国大陆

  • T70860Banoxantrone；化合物 Banoxantrone (AQ4N)AQ4N；AQ4N

    Banoxantrone (AQ4N), a hypoxia-selective cytotoxin prototype, undergoes reduction to AQ4, effectively inhibiting topoisomerase II. It selectively targets and eradicates hypoxic cells through an iNOS-dependent mechanism. This compound demonstrates significant cytotoxicity with its hypoxia-selective action being augmented by radiation.

    价 格：￥电议型 号：T70860产 地：中国大陆

  • T70797AQ-RA 721；化合物 AQ-RA 721AQ-RA 721

    AQ-RA 721 is a selective muscarinic antagonist with high affinity for M1- and M3-receptors. AQ-RA 721 may be used as a bronchodilator.

    价 格：￥电议型 号：T70797产 地：中国大陆

  • T70715AQW-051 fumarate；化合物 AQW-051 fumarateAQW-051 fumarate

    AQW-051 fumarate is an α7 nicotinic ACh receptor partial agonist that may act as a cognitive-enhancing agent.

    价 格：￥电议型 号：T70715产 地：中国大陆

  • T7035ANTHRAQUINONE-2-CARBOXYLIC ACID；蒽醌-2-羧酸ANTHRAQUINONE-2-CARBOXYLIC ACID

    Anthraquinone-2-carboxylic acid acts as a potent anti-inflammatory and antinociceptive component in vivo, thus contributing to the immune regulatory role of fruits and herbs.

    价 格：￥电议型 号：T7035产 地：中国大陆

  • T70197AQ 148；化合物 AQ 148AQ 148

    AQ 148 is a potent competitive inhibitor of HIV-1 PR.

    价 格：￥电议型 号：T70197产 地：中国大陆

  • T69906PEAQX sodium；化合物 PEAQX sodiumPEAQX sodium

    PEAQX, also known as NVP-AAM077; is a competitive antagonist at the NMDA receptor. Although originally described as 100-fold selective for GluN1/GluN2A receptors vs. GluN1/GluN2B receptors, more detailed studies of the Ki of PEAQX revealed it only shows a 5 fold difference in affinity for GluN1/GluN2A vs. GluN1/GluN2B receptors. It is also a potent anticonvulsant in animal tests.

    价 格：￥电议型 号：T69906产 地：中国大陆

  • T69569Aquayamycin；化合物 AquayamycinAquayamycin

    Aquayamycin is an anthraquinone derivative and inhibitor of the enzyme tyrosine hydroxylase..

    价 格：￥电议型 号：T69569产 地：中国大陆

11234567891012下一页共12页

展台首页| 公司简介| 供应产品| 产品目录| 公司动态| 荣誉证书| 招聘信息| 技术中心| 联系我们| 会员管理

易推广  设计制作，未经允许翻录必究.Copyright(C) 2009 http://www.yituig.com, All rights reserved.

以上信息由企业自行提供，信息内容的真实性、准确性和合法性由相关企业负责，易推广对此不承担任何责任.   总访问量：3691640

中国彩虹热线

快速导航

返回顶部
在线咨询

提交